BeNa Culture Collection
info@bncc.com
| Subculture procedure | ① Prepare 2 tablets; ② Open the safety cabinet, burn the top with an alcohol lamp, quickly drip sterile water to break it, and then use tweezers to crush it; ③ Take 0.5mL of sterile water and pour it into the freeze-drying tube. After fully dissolving, mix well; ④ Transfer 0.2mL of bacterial suspension into a Agar plate, apply evenly, and repeat twice to obtain two plates; ⑤ Place all the plates under the above cultivation conditions, and once the strains grow, they can be used. |
| Growth conditions | 28 ℃, 5-7 days, aerobic |
| Storage conditions | 2-8 ℃ |
| Safety level | 1 |
| morphology | Filamentous, spreading and growing, producing yellow spores |
| Sharing mode | Public welfare sharing |
Aspergillus oryzae
BNCC No.: 195382
Storage conditions: 2~8 ℃
Product format: freeze dried, 200ul
Validity period: 6 years
Biosafety level: 1, handle in ultra-clear table or safety cabinet
Receiving notice: if any abnormality is found on the day of receipt, please contact the customer service within 24 hours. If it is overdue, it is deemed that the bacteria are well. The freeze dried culture shall be used up once and shall not be retained. The bacterial viability will resume after 1-2 generation of recovery and can be used normally. Handling instructions of agar slant and suspension liquid is enclosed. Please operate in strict accordance with this instruction, otherwise the replacement of bacteria are not be available in case of aberrant growth and loss of viability.
Growth conditions:25-28 ℃, aerobic, integrated PDA agar, 3-7 days. Comprehensive PDA agar: potato boil 1.0L, glucose 20.0g,KH2PO4 3.0g,MgSO4.7H2O 1.5g, vitamin B1 trace, agar 20.0g,pH 6.0±0.2. Sterilization at 121 ℃ for 15min. Potato boiling liquid: weigh 200g of peeled potato pieces, boil in boiling water for 30min, and collect the filtrate to a constant volume of 1.0L.
Recovery steps:
(1)Prepare 2 plates;
(2) Open it in the biosafety cabinet, heat the tip of ampoule in a flame, quickly drop sterile water to creak it, then break it with forceps;
(3) Draw 0.5mL of liquid culture medium into a freeze dried ampoule, fully rehydrate and transfer the solution to the liquid test tube, mix evenly;
(4) Inoculate a plate with 0.2mL of suspension liquid, repeat the step to obtain two plates;
(5) Put all the liquid test tubes and plates under the above culture conditions for cultivation, and the strains can be used when they grow.
Recovery record: According to the recovery instructions, the results of the recovery are reported as follows:

| item | test results |
| viability: | good viability,in 3-7 days plate colony is obvious, |
| colony morphology: |
small filamentous fungi have obvious colonies on comprehensive PDA medium, and the colonies are white at first, After turning to yellow-green, the surface is fluffy, producing yellow-green spores, and the back is light khaki |
| conclusion: | good viability, no abnormal colony morphology, qualified |